Does CAPECITABINE Cause Product prescribing error? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product prescribing error have been filed in association with CAPECITABINE (Capecitabine). This represents 0.0% of all adverse event reports for CAPECITABINE.
28
Reports of Product prescribing error with CAPECITABINE
0.0%
of all CAPECITABINE reports
3
Deaths
13
Hospitalizations
How Dangerous Is Product prescribing error From CAPECITABINE?
Of the 28 reports, 3 (10.7%) resulted in death, 13 (46.4%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPECITABINE. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does CAPECITABINE Cause?
Diarrhoea (9,277)
Nausea (6,248)
Palmar-plantar erythrodysaesthesia syndrome (5,294)
Fatigue (5,018)
Death (4,422)
Vomiting (4,111)
Disease progression (3,808)
Off label use (3,193)
Malignant neoplasm progression (2,425)
Asthenia (2,352)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which CAPECITABINE Alternatives Have Lower Product prescribing error Risk?
CAPECITABINE vs CAPIVASERTIB
CAPECITABINE vs CAPLACIZUMAB
CAPECITABINE vs CAPLACIZUMAB-YHDP
CAPECITABINE vs CAPMATINIB
CAPECITABINE vs CAPREOMYCIN